Supervisor, Study Services

Champions Oncology, Inc.

Rockville (MD)

On-site

USD 90,000 - 120,000

Full time

14 days+

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Job summary

Champions Oncology, Inc. in Rockville, MD is seeking a Supervisor of Study Services to lead a small team of technicians and assistants, coordinate with cross-functional groups, and ensure timely study initiation and data integrity.

You will supervise staff, conduct competency assessments, mentor team members, review protocols, and oversee in-life procedures, perioperative care, and data capture in LIMS. The role requires a BS/MS in biology or pharmacology or 5+ years related experience, 1 year

Qualifications

  • BS/MS in biology, pharmacology, or related field, or minimum of 5 years related experience.
  • At least 1 year supervisory or management experience.
  • Experience in contract research animal facility or industry setting preferred.
  • AAALAS certification preferred (LAT or LATG).

Responsibilities

  • Hire and manage small teams of technicians, apprentices, and assistants within Study Services, including competency assessments and skill development plans.
  • Coordinate with cross-functional groups, management, and Project Leadership.
  • Review draft and final protocols, extract relevant information and assign responsibilities to staff, including study initiation and cross company coordination.
  • Evaluate, train, and mentor staff, including review of daily work task completion and monthly metrics.
  • Lead weekly and daily meetings to ensure task completion in a timely manner.
  • Improve procedures and processes and investigate deviations and near-misses.
  • Create, review, and edit Standard Operating Procedures (SOPs) and processes.
  • May act as lead technician on studies.
  • Perform in-life technical procedures, therapeutic agent administration, and care for all animals.
  • Provide animal welfare assessments, including body weight and tumor volume measurement.
  • Provide perioperative animal care, including analgesia and anesthesia administration.
  • Record data using laboratory information management systems.
  • Work weekends and holidays on a rotating basis.

Skills

Preclinical in vivo studies
Data analysis
Team leadership
Problem solving
Planning & organization
Safety/compliance AAALAC/CLIA
Adaptability
Written/verbal communication

Education

BS/MS in biology/pharmacology
5+ years related experience
Supervisory/management experience
AAALAS LAT/LATG preferred

Job description

Title and Classification

Supervisor, Study Services

Reporting Location

Rockville, MD

Reports To

Director, Laboratory Operations

Primary Objectives

Support in vivo oncology studies in mice as a Supervisor of Study Services. Directly manage staff. Responsible for providing leadership to the Study Services Team and interfacing with cross company teams.

Duties and Responsibilities
  • Hire and manage small teams of technicians, apprentices, and assistants within Study Services, including competency assessments and skill development plans.
  • Coordinate with cross-functional groups, management, and Project Leadership.
  • Review draft and final protocols, extract relevant information and assign responsibilities to staff, including study initiation and cross company coordination.
  • Evaluate, train, and mentor staff, including review of daily work task completion and monthly metrics.
  • Lead weekly and daily meetings to ensure task completion in a timely manner.
  • Improve procedures and processes and investigate deviations and near-misses.
  • Create, review, and edit Standard Operating Procedures (SOPs) and processes.
  • May act as lead technician on studies.
  • Perform in-life technical procedures, therapeutic agent administration, and care for all animals.
  • Provide animal welfare assessments, including body weight and tumor volume measurement.
  • Provide perioperative animal care, including analgesia and anesthesia administration.
  • Record data using laboratory information management systems.
  • Work weekends and holidays on a rotating basis.
Knowledge, Skills, and Abilities
  • Experience with preclinical in vivo pharmacology or oncology studies in mice.
  • Technical in vivo and data analysis skills.
  • Ability to work effectively and productively in a team-oriented environment while maintaining a strong sense of accountability, integrity, and confidentiality.
  • Creative problem-solving skills and the ability to exercise sound and accurate judgment in making timely decisions.
  • Superior planning, organizational, computer, written, and verbal communication skills.
  • Ability to assist with other duties in a dynamic environment.
  • Understanding of animal welfare and clinical testing regulations and standards (e.g., AAALAC, CLIA).
  • Ability to observe safety and security procedures.
Education and Experience
  • BS/MS degree in biology, pharmacology, or related field, or minimum of 5 years of related experience.
  • At least 1 year supervisory or management experience.
  • Experience in contract research animal facility or industry setting is preferred.
  • AAALAS certification preferred (LAT or preferably LATG).
Physical Demands and Work Environment
  • Must be able to sit and use hands to finger, handle and feel.
  • Must be able to lift and move packages weighing up to 50 pounds.
  • Must be able to sit for long periods of time using a computer in a typical office environment in a multi-level facility.
  • Some activities require repetitive motion and reaching, pulling, or pushing.
  • In carrying out the duties of the job there will be frequent exposure to fumes and chemical hazards.
  • Duties performed routinely require exposure to blood, body fluid and tissue.

This description reflects management’s assignment of essential functions, it does not proscribe or restrict the tasks that may be assigned. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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